Prev Term: autosomal dominant trait
Next Term: autosome
autosomal recessive trait
Broader Terms:
phenotype
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abetalipoproteinemia
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acrodermatitis enteropathica
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alpha 1 antitrypsin deficiency
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argininemia
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arginosuccinate lyase deficiency
Related Terms:
arginosuccinate synthetase deficiency
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Bartter's syndrome
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Bloom syndrome
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cerebrohepatorenal syndrome
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cerebrotendinous xanthomatosis
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Chediak Higashi syndrome
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congenital erythropoietic porphyria
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cystic fibrosis
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fucosidosis
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Gaucher's disease
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happy puppet syndrome
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hepatolenticular degeneration
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hereditary fructose intolerance
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hereditary hemochromatosis
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histidinemia
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homocystinuria
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hyperglycinemia
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hyperphenylalaninemia
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I cell disease
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isovaleric acidemia
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maple syrup urine disease
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metachromatic leukodystrophy
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methylmalonic aciduria
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mucopolysaccharidosis type I
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Nijmegen breakage syndrome
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phenylketonuria
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pyruvate kinase deficiency
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Refsum disease
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Smith Lemli Opitz syndrome
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Tangier disease
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Tay Sachs disease
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Usher syndrome
Related Terms:
Werner's syndrome
Related Terms:
xeroderma pigmentosum
Scope Note:
trait expressed when the responsible allele is carried by both members of a pair of homologous autosomes.
Term Number:
1254-7856
Send your comments to: Melody Lowe